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CODEX: a normalization and copy number variation detection method for whole exome sequencing
High-throughput sequencing of DNA coding regions has become a common way of assaying genomic variation in the study of human diseases. Copy number variation (CNV) is an important type of genomic variation, but detecting and characterizing CNV from exome sequencing is challenging due to the high leve...
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| 發表在: | Nucleic Acids Res |
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| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4381046/ https://ncbi.nlm.nih.gov/pubmed/25618849 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gku1363 |
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